Transgenic Mouse/Embryonic Stem Cell Shared Resource: Project Summary/Abstract For the past 22 years, the Transgenic Mouse/Embryonic Stem Cell Shared Resource (TMESCSR) has provided a cornerstone for many scientific advances within the Vanderbilt Diabetes Research and Training Center (VDRTC), and elsewhere. Not only have the TMESCSR-derived mice enabled hundreds of highly impactful studies to be performed by VDRTC investigators, they have also been utilized by numerous other non-VDRTC investigators who obtain these animals from public repositories. With the discovery of CRISPR/Cas, which enables the derivation of mice with precisely targeted mutations in a rapid and efficient manner, the TMESCSR made the strategic decision to discontinue its long-standing mouse ES cell (mESC)- based gene targeting service. This action enabled the personnel supporting this resource to optimize and deliver a new CRISPR/Cas-based service, while continuing to provide many other frequently utilized mouse- based services. Together, the services provided by the TMESCSR enable VDRTC members to efficiently derive mice with new genetic alterations, to maintain and cryopreserve existing mouse lines, and to derive new lines from the vast number of mutant mESCs and frozen embryos or sperm that are now available from several large-scale mutagenesis projects, including the Knock-out Mouse Project (KOMP). VDRTC support enables the TMESCSR to import and optimize new technology, such as CRISPR/Cas, thereby assuring that VDRTC investigators have continuing access to up-to-date strategies for deriving state-of-the-art mouse models. These mouse models, in turn, enable VDRTC members to perform high quality studies to understand the pathogenesis of diabetes, obesity and other endocrine diseases, and to perform preclinical testing of new therapies for these diseases, utilizing the expertise in other VDRTC-supported cores (e.g. Cell Imaging Shared Resource, Metabolic Physiology Shared Resource, Hormone Assay and Analytical Services Core).

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK020593-43
Application #
9933896
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
43
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
DUNS #
079917897
City
Nashville
State
TN
Country
United States
Zip Code
37232
Kovtun, Oleg; Tomlinson, Ian D; Bailey, Danielle M et al. (2018) Single Quantum Dot Tracking Illuminates Neuroscience at the Nanoscale. Chem Phys Lett 706:741-752
Marks, Christian R; Shonesy, Brian C; Wang, Xiaohan et al. (2018) Activated CaMKII? Binds to the mGlu5 Metabotropic Glutamate Receptor and Modulates Calcium Mobilization. Mol Pharmacol 94:1352-1362
Burke, Susan J; Batdorf, Heidi M; Burk, David H et al. (2018) Pancreatic deletion of the interleukin-1 receptor disrupts whole body glucose homeostasis and promotes islet ?-cell de-differentiation. Mol Metab :
Coppola, Jennifer J; Disney, Anita A (2018) Most calbindin-immunoreactive neurons, but few calretinin-immunoreactive neurons, express the m1 acetylcholine receptor in the middle temporal visual area of the macaque monkey. Brain Behav 8:e01071
Choksi, Yash A; Reddy, Vishruth K; Singh, Kshipra et al. (2018) BVES is required for maintenance of colonic epithelial integrity in experimental colitis by modifying intestinal permeability. Mucosal Immunol 11:1363-1374
Zhu, Lin; Luu, Thao; Emfinger, Christopher H et al. (2018) CETP Inhibition Improves HDL Function but Leads to Fatty Liver and Insulin Resistance in CETP-Expressing Transgenic Mice on a High-Fat Diet. Diabetes 67:2494-2506
Shropshire, J Dylan; On, Jungmin; Layton, Emily M et al. (2018) One prophage WO gene rescues cytoplasmic incompatibility in Drosophila melanogaster. Proc Natl Acad Sci U S A 115:4987-4991
Lu, Sichang; McGough, Madison A P; Shiels, Stefanie M et al. (2018) Settable polymer/ceramic composite bone grafts stabilize weight-bearing tibial plateau slot defects and integrate with host bone in an ovine model. Biomaterials 179:29-45
Brissova, Marcela; Haliyur, Rachana; Saunders, Diane et al. (2018) ? Cell Function and Gene Expression Are Compromised in Type 1 Diabetes. Cell Rep 22:2667-2676
Kook, Seunghyi; Qi, Aidong; Wang, Ping et al. (2018) Gene-edited MLE-15 Cells as a Model for the Hermansky-Pudlak Syndromes. Am J Respir Cell Mol Biol 58:566-574

Showing the most recent 10 out of 697 publications